Canonical Allele Identifier: CA1814482854
Gene: TNFRSF11B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947734_118947735delinsTA , CM000670.2:g.118947734_118947735delinsTA GRCh38
NC_000008.10:g.119959973_119959974delinsTA , CM000670.1:g.119959973_119959974delinsTA GRCh37
NC_000008.9:g.120029154_120029155delinsTA NCBI36
NG_012202.1:g.9410_9411delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.30+4057_30+4058delinsTA MANE Select ENSP00000297350.4:n.30+4057_30+4058delinsTA
ENST00000297350.8:c.30+4057_30+4058delinsTA ENSP00000297350.4:n.30+4057_30+4058delinsTA
ENST00000517352.1:c.30+4057_30+4058delinsTA ENSP00000427924.1:n.30+4057_30+4058delinsTA
NM_002546.3:c.30+4057_30+4058delinsTA NP_002537.3:n.30+4057_30+4058delinsTA
NM_002546.4:c.30+4057_30+4058delinsTA MANE Select NP_002537.3:n.30+4057_30+4058delinsTA
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